Haim Munk syndrome 719973009
SNOMED CT code
| SNOMED code | 719973009 |
|---|---|
| name | Haim Munk syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Haim Munk syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Skin structure 39937001 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group4 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Tooth structure 38199008 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Skin structure 39937001 |
| Associated morphology | Hyperkeratosis 26996000 |
| attributes - group3 | |
| Associated morphology | Hyperkeratosis 26996000 |
| Finding site | Entire skin of palmar area of hand 181544004 |
| attributes - group5 | |
| Finding site | Entire skin of sole of foot 181566006 |
| Associated morphology | Hyperkeratosis 26996000 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Hereditary disorder of tooth 1148766007 Haim Munk syndrome 719973009 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Haim Munk syndrome 719973009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Haim Munk syndrome 719973009 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Hereditary palmoplantar keratoderma 239066003 Hereditary diffuse palmoplantar keratoderma 400123002 Haim Munk syndrome 719973009 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of mouth region 423066003 Oral cavity finding 116337000 Congenital abnormality of oral cavity 282041002 Congenital anomaly of tooth 422977003 Haim Munk syndrome 719973009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Haim Munk syndrome 719973009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Haim Munk syndrome 719973009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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